Dental C-Patch

Manufacturer
NeoBiotech Global Corporation
Effective date
2018-02-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:54:27

Label at a glance#

ProductDental C-Patch
Active ingredientCAMPHOR (SYNTHETIC), MENTHOL
Label structure8 sections

Indications and uses

temporarily relieves symptoms of - discomfort after dental procedure - inflammation - minor irritation - swelling

Dosage and administration

Adults and children over 12 years: - remove film from patch - carefully apply the patch to the affected skin over the area of ental procedure - press patch onto skin firmly - patch can remain on the skin for up to 8 hours - may repeat as necessary up to 3 times per day

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Camphor (0.5%)

Menthol (2.5%)

Purpose

OTC - PURPOSE SECTION

External analgesic

Uses

INDICATIONS & USAGE SECTION

temporarily relieves symptoms of

- discomfort after dental procedure

- inflammation

- minor irritation

- swelling

Warnings

WARNINGS SECTION

For external use only

When using this product

Use only as directed.

- Do not bandage tightly or use with heating pad

- Avoid contact with eyes and mucus membranes

- Do not appy wounds or broken skin

- Do not apply to large areas of the body

- In case of deep or puncture wounds, animal bites or serious burns, consult a doctor

Stop use and ask a doctor if

- condition worsen

- irritation develops

- symptoms persist for more than 7 days or recurs within 1 day of discontinuation

- do not use for more than 7 days

If pregnant or breast-feeding, ask a health professional before use

Keep out of reach of children. If swallowd, contact a Poison Control Center or get medical help immediatel

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children over 12 years:

- remove film from patch

- carefully apply the patch to the affected skin over the area of ental procedure

- press patch onto skin firmly

- patch can remain on the skin for up to 8 hours

- may repeat as necessary up to 3 times per day

Inactive ingredients

INACTIVE INGREDIENT SECTION

Charcoal, gelatin, Aluminum glycinate, Ethylenediaminetetraacetic acid, disodium slat, eucalyptus oil, glycerin, polyvlnyl alcohol, partially neutralized polyacrytate, pured wter, salt, sorbitol, tartaric acid

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, contact a Poison Control Center or get medical help immediately

Dental C-Patch

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

dental c-patchdental c-patch

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1997510camphor 0.5 % / menthol 2.5 % Medicated PatchPSN2
1997510camphor 0.005 MG/MG / menthol 0.025 MG/MG Medicated PatchSCD2
1997510camphor 0.5 % / menthol 2.5 % Medicated PatchSY2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
777d68c6-a5ab-e06c-d314-677b0b9af0c8Product name220240508
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70236-104-022020-01-31C16284748780-19d75b9d1-188d-f424-e053-dadaa90a57ceDental C-Patch

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70236-104-01Dental C-Patch14 g in 1 PATCHPATCH142
70236-104-02Dental C-Patch5 in 1 POUCHPATCH52

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70236-104DENTAL C-PATCH (MENTHOL, CAMPHOR) PATCH [NEOBIOTECH GLOBAL CORPORATION]2Legacy NDC, 2 package rows20180210_64dd06d5-da2e-3a74-e053-2a91aa0a6d3b.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70236-10470236-104-01, 70236-104-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
64dd06d5-da2f-3a74-e053-2a91aa0a6d3b64dd06d5-da2e-3a74-e053-2a91aa0a6d3b2018-02-10WarningsExact identifier
spl id: 64dd06d5-da2f-3a74-e053-2a91aa0a6d3b
spl set id: 64dd06d5-da2e-3a74-e053-2a91aa0a6d3b

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.